A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6443102



Internal ID21100655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:98392999..98393387hg38UCSC Ensembl
chr9:101155281..101155669hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg38389
hg19389
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18219051
Samples
Known GenesGABBR2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6443102
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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